Lam Marissa, Lum Caroline, Latham Sarah, Tipping Smith Sam, Prenen Hans, Segelov Eva
Department of Medical Oncology, Monash Medical Center, Clayton, Australia.
Department of Oncology, University Hospital Antwerp, Edegem, Belgium.
Cancer Manag Res. 2020 Jul 15;12:5819-5830. doi: 10.2147/CMAR.S213236. eCollection 2020.
Despite advances, patients with metastatic colorectal cancer (mCRC) still have poor long-term survival. Identification of molecular subtypes is important to guide therapy through standard treatment pathways and holds promise for the development of new treatments. Following standard first- and second-line chemotherapy plus targeted agents, many patients retain a reasonable performance status, and thus are seeking further effective treatment to extend life and maintain symptom control. The challenge lies in selecting the most appropriate therapy in the third- and fourth-line settings, from a range of options including the relatively new oral agents TAS-102 and regorafenib, or rechallenge with previous chemotherapy or anti-epidermal growth factor receptor (anti-EGFR) monoclonal antibodies (mAB). Beyond this, therapy consists of trials involving novel agents and new combinations of treatments with theoretical synergy and/or non-overlapping toxicity. There is a great focus on enhancing immunogenicity in mCRC, to reflect the impressive results of immunotherapy drugs in the small cohort with mismatch repair deficient (dMMR) mCRC. Rare molecular subtypes of mCRC are increasingly being identified, including -positive disease, fusions and others. Clinical trials exploring the efficacy of immunomodulatory and precision agents are plentiful and will hopefully yield clinically meaningful results that can be rapidly translated into routine care.
尽管取得了进展,但转移性结直肠癌(mCRC)患者的长期生存率仍然很低。识别分子亚型对于通过标准治疗途径指导治疗很重要,并且有望开发新的治疗方法。在接受标准的一线和二线化疗加靶向药物治疗后,许多患者仍保持合理的身体状况,因此正在寻求进一步的有效治疗以延长生命并维持症状控制。挑战在于在三线和四线治疗中,从一系列选择中选择最合适的治疗方法,这些选择包括相对较新的口服药物TAS-102和瑞戈非尼,或重新使用先前的化疗药物或抗表皮生长因子受体(anti-EGFR)单克隆抗体(mAB)。除此之外,治疗还包括涉及新型药物以及具有理论协同作用和/或非重叠毒性的新治疗组合的试验。人们非常关注增强mCRC的免疫原性,以反映免疫治疗药物在错配修复缺陷(dMMR)mCRC小队列中的令人印象深刻的结果。越来越多的mCRC罕见分子亚型被发现,包括 -阳性疾病、融合等。探索免疫调节和精准药物疗效的临床试验很多,有望产生具有临床意义的结果,并能迅速转化为常规治疗。